Evidence map›Paper›PMID 31247475›Full record

ArticleEpilepsy research2019

Synthetic aperture magnetometry and excess kurtosis mapping of Magnetoencephalography (MEG) is predictive of epilepsy surgical outcome in a large pediatric cohort.

J S Gofshteyn, T Le, S Kessler, R Kamens, C Carr, W Gaetz, L Bloy, T P L Roberts, E S Schwartz, E D Marsh

Open access · greenAbstract read
In one paragraph

Article in Epilepsy research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

J S GofshteynDivision of Pediatric Neurology, Department of Pediatrics, Weill Cornell Medicine, New York, NY, United States; New-York Presbyterian Hospital, New York, NY, United States.
T LeDivision of Pediatric Neurology, The Children's Hospital of Philadelphia, United States.
S KesslerDivision of Pediatric Neurology, The Children's Hospital of Philadelphia, United States; Departments of Neurology and Pediatrics, Perelman School of Medicine at the University of Pennsylvania, United States.
R KamensDivision of Pediatric Neurology, The Children's Hospital of Philadelphia, United States.
C CarrDivision of Pediatric Neurology, The Children's Hospital of Philadelphia, United States.
W GaetzDivision of Neuroradiology, Department of Radiology, The Children's Hospital of Philadelphia, United States; Department of Radiology, Perelman School of Medicine at the University of Pennsylvania, United States.
L BloyDivision of Neuroradiology, Department of Radiology, The Children's Hospital of Philadelphia, United States; Department of Radiology, Perelman School of Medicine at the University of Pennsylvania, United States.
T P L RobertsDivision of Neuroradiology, Department of Radiology, The Children's Hospital of Philadelphia, United States; Department of Radiology, Perelman School of Medicine at the University of Pennsylvania, United States.
E S SchwartzDivision of Neuroradiology, Department of Radiology, The Children's Hospital of Philadelphia, United States; Department of Radiology, Perelman School of Medicine at the University of Pennsylvania, United States.
E D MarshDivision of Pediatric Neurology, The Children's Hospital of Philadelphia, United States; Departments of Neurology and Pediatrics, Perelman School of Medicine at the University of Pennsylvania, United States. Electronic address: marshe@email.chop.edu.
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · USCornell University · US

Funding

The Intellectual and Developmental Disabilities Research Center at CHOP/PennU54HD086984 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI SCHULTZ, ROBERT THOMAS · 2016 to 2020
$6.3M
Electrophysiological Signatures of Language Impairment in Autism Spectrum DisordeR01DC008871 · NIDCD · CHILDREN'S HOSP OF PHILADELPHIA · PI ROBERTS, TIMOTHY P · 2007 to 2018
$3.6M
Virtual Resection to Treat EpilepsyR01NS099348 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI BASSETT, DANIELLE SMITH, LITT, BRIAN · 2016 to 2019
$2.3M
Neurophysiological and neuroanatomical processes related to Autism Spectrum Disorder in Neurofibromatosis Type 1R21NS106135 · NINDS · CHILDREN'S HOSP OF PHILADELPHIA · PI HOCKING, MATTHEW C., ROBERTS, TIMOTHY P · 2018 to 2019
$473k
NICHD NIH HHS U54 HD086984NIDCD NIH HHS R01 DC008871NINDS NIH HHS R01 NS099348NINDS NIH HHS R21 NS106135
6 · The paper itself

Abstract

objectiveResective surgery is the most effective treatment option for patients with refractory epilepsy; however identification of patients who will benefit from epilepsy surgery remains challenging. Synthetic aperture magnetometry and excess kurtosis mapping (SAM(g2)) of magnetoencephalography (MEG) is a non-invasive tool that warrants further examination in the pediatric epilepsy population. Here, we examined the utility of MEG with SAM(g2) to determine if MEG epileptiform foci correlates with surgical outcome and to develop a predictive model incorporating MEG information to best assess likelihood of seizure improvement/freedom from resective surgery.

methods564 subjects who had MEG at the Children's Hospital of Philadelphia between 2010-2015 were screened. Clinical epilepsy history and prior electrographic records were extracted and reviewed and correlated with MEG findings. MEG assessments were made by both a neurologist and neuroradiologist. Predictive models were developed to assess the utility of MEG in determining Engel class at one year and five years after resective epilepsy surgery.

resultsThe number of MEG spike foci was highly associated with Engel class outcome at both one year and five years; however, using MEG data in isolation was not significantly predictive of 5 year surgical outcome. When combined with clinical factors; scalp EEG (single ictal onset zone), MRI (lesional or not), age and sex in a logistic regression model MEG foci was significant for Engel class outcome at both 1 year (p = 0.03) and 5 years (0.02). The percent correctly classified for Engel class at one year was 78.43% and the positive predictive value was 71.43. SIGNIFICANCE: MEG using SAM(g2) analysis in an important non-invasive tool in the identification of those patients who will benefit most from surgery. Integrating MEG data analysis into pre-surgical evaluation can help to predict epilepsy outcome after resective surgery in the pediatric population if utilized with skilled interpretation.

Indexed as

AdolescentBrainChildChild, PreschoolEpilepsyFemaleHumansMagnetoencephalographyMagnetometryMaleNeurosurgical ProceduresPrognosisRetrospective StudiesTreatment OutcomeEngel classEpilepsy surgeryMagnetoencephalographyPediatric epilepsySynthetic aperture magnetometry

Identifiers

PMID31247475
PMCPMC6699633
OpenAlexW2952852099

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.